HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615377Generated: October 31, 2026
2-Piperidone → 4-{[2-(1,4-Benzodioxan-2-yl)-2-hydroxyethyl]amino}piperidine
https://huagongshe.com/reaction/615377
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 13121298 | HCID 13121298 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-{[2-(1,4-Benzodioxan-2-yl)-2-hydroxyethyl]amino}piperidine | HCID 20427768 | — |
Reaction Steps
The [2-(1,4-benzodioxan-2-yl)-2-hydroxyethyl]amine prepared in Preparation A' (50 g) and piperidone (85 g) are dissolved in 500 ml of ethanol. Seventy-five grams of sodium cyanoborohydride is added, and the mixture is maintained at room temperature for 12 hours and cooled and evaporated. The product is recovered by adding aqueous ammonia to the residue and extracting with methylene chloride. Three 100 ml portions of methylene chloride are used which are combined, washed twice with 50 ml of water and evaporated to a semi-solid. Upon addition of ether, the product crystallizes and is recovered by filtration. The resulting crude mixture is boiled gently in 100 ml of diethyl ether and then evaporated to a residue and triturated with hexane to yield pure material, 4-{[2-(1,4-benzodioxan-2-yl)-2-hydroxyethyl]amino}piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499100 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-281c5b70721046bb917de6383b3951e7 |
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| Source note | uspto-grants-1985_02 |
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